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PubMed:27794539 / 125-321 JSONTXT

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c_corpus

Id Subject Object Predicate Lexical cue
T27 13-20 6308 denotes leucine
T28 13-20 SO:0001437 denotes leucine
T26 13-20 CHEBI:15603 denotes leucine
T29 13-20 D007930 denotes leucine
T30 13-20 CHEBI:25017 denotes leucine
T31 13-20 D007930 denotes leucine
T32 26-32 SO:0001068 denotes repeat
T33 43-48 PR:Q5S006 denotes LRRK2
T34 43-48 PR:000003033 denotes LRRK2
T35 43-48 PR:Q5S007 denotes LRRK2
T36 56-66 D000067562 denotes late-onset
T37 56-66 D000067562 denotes late-onset
T38 68-86 C566739 denotes autosomal dominant
T43 96-115 D010300 denotes Parkinson`s disease
T44 96-115 D010300 denotes Parkinson`s disease
T47 142-147 PR:Q5S006 denotes LRRK2
T48 142-147 PR:000003033 denotes LRRK2
T49 142-147 PR:Q5S007 denotes LRRK2

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 0-196 DRI_Approach denotes Mutations in leucine-rich repeat kinase 2 (LRRK2) cause late-onset, autosomal dominant familial Parkinson`s disease (PD) and variation at the LRRK2 locus contributes to the risk for idiopathic PD.